FDA 510(k) Applications Submitted by Annette Minthorn
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191238 | 05/08/2019 | Zimmer Guide Wire Devices | Zimmer, Inc |
| K173826 | 12/18/2017 | THP Hip Fracture Plating System | Biomet, Inc. |
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